Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs2430561
IFNG ; IFNG-AS1
0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs56149945
NR3C1
0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 49
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs324981
NPSR1-AS1 ; NPSR1
0.724 0.320 7 34778501 missense variant A/T snv 0.44 0.47 18
rs1861494
IFNG-AS1 ; IFNG
0.716 0.400 12 68157629 intron variant C/T snv 0.75 15
rs110402
CRHR1 ; LINC02210-CRHR1 ; MAPT-AS1
0.790 0.120 17 45802681 intron variant G/A;C snv 12
rs1143643
IL1B
0.790 0.320 2 112830725 intron variant C/T snv 0.29 10
rs439401 0.851 0.200 19 44911194 non coding transcript exon variant T/C snv 0.68 8
rs222747
TRPV1
0.827 0.240 17 3589906 missense variant C/A;G;T snv 0.72; 4.5E-06 8
rs1799722
BDKRB2
0.882 0.240 14 96204802 5 prime UTR variant C/T snv 0.41 0.39 4
rs2228305
FASN
0.925 0.120 17 82084916 missense variant C/T snv 4.1E-02 4.5E-02 3
rs5479
HSD11B2
0.925 0.080 16 67435830 synonymous variant C/A;G;T snv 5.4E-02; 8.0E-06; 4.0E-06 3
rs145579007
ACE
0.925 0.080 17 63496503 missense variant G/A snv 1.0E-04 1.0E-04 2
rs750712925
ACE
0.925 0.080 17 63477227 missense variant G/A;C;T snv 3.2E-05 2
rs56303414
HSD11B2
0.925 0.080 16 67432532 intron variant C/G snv 0.55 2
rs3087879
SLC1A1 ; SPATA6L
0.925 0.080 9 4586808 3 prime UTR variant G/C snv 0.28 2
rs3792738
CRHBP ; S100Z
1.000 0.040 5 76951959 upstream gene variant C/A;G snv 1